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Inter-laboratory ring trials to evaluate serological methods for dourine diagnosis
Julien Cauchard1, Andrew Soldan2, Anthony Madeline1
1ANSES, Dozulé laboratory for equine diseases, Bacteriology and Parasitology Unit, Goustranville, France.
Veterinary Parasitology
|July 13, 2014
Summary
This study assessed dourine serological tests, finding the complement fixation test (CFT) reliable for Trypanosoma equiperdum. However, specificity issues arose with Trypanosoma evansi cross-reactivity, suggesting reagent standardization is needed.
Area of Science:
- Veterinary Immunology
- Parasitology
- Diagnostic Serology
Background:
- Dourine, caused by Trypanosoma equiperdum, is a significant equine disease.
- Accurate serological diagnosis is crucial for disease control and eradication efforts.
- Inter-laboratory reproducibility of diagnostic tests is essential for reliable disease surveillance.
Purpose of the Study:
- To evaluate the reproducibility of routine serological methods for Trypanosoma equiperdum antibody detection in equine sera.
- To assess the performance of the complement fixation test (CFT) and indirect fluorescent antibody test (IFAT) in a ring trial setting.
- To identify potential sources of variability and suggest improvements for dourine serodiagnosis.
Main Methods:
- Two inter-laboratory ring trials were conducted with 26 laboratories (22 European, 4 non-European).
- Laboratories applied the complement fixation test (CFT) and/or indirect fluorescent antibody test (IFAT).
- Sample panels included sera negative, positive, or suspected for dourine, and one serum positive for Trypanosoma evansi.
Main Results:
- The CFT demonstrated good inter-laboratory reproducibility for known Trypanosoma equiperdum positive and negative sera.
- False-positive results were observed in nine laboratories when testing a Trypanosoma evansi-positive serum using CFT or IFAT.
- Seropositivity was confirmed in one of three horses initially suspected of dourine.
Conclusions:
- The CFT is a reliable method for dourine serodiagnosis, but its specificity can be compromised by cross-reactivity with Trypanosoma evansi.
- Standardizing critical reagents, such as antigens and developing a standard Trypanosoma equiperdum serum, could improve diagnostic specificity.
- Implementing a standardized low-titer serum control is recommended to ensure consistent test sensitivity across laboratories.

